Search results for "Perylene"

showing 10 items of 70 documents

Quantum Chemical Parametrization and Spectroscopic Characterization of the Frenkel Exciton Hamiltonian for a J-Aggregate Forming Perylene Bisimide Dye

2012

Quantum chemical and quantum dynamical calculations are performed for a bay-substituted perylene bisimide dye up to its hexameric aggregate. The aggregate structure is determined by employing the self-consistent charge density functional tight-binding (SCC-DFTB) approach including dispersion corrections. It is characterized by a stabilization via two chains of hydrogen bonds facilitated by amide functionalities. Focusing on the central embedded dimer, the Coulomb coupling for this J-aggregate is determined by means of the time-dependent density functional theory (TDDFT) to be -514 cm(-1). Exciton vibrational coupling is treated within the shifted oscillator model from which five strongly co…

Molecular StructureAbsorption spectroscopyChemistryExcitonCharge densityTime-dependent density functional theoryImideschemistry.chemical_compoundQuantum TheoryDensity functional theoryPhysical and Theoretical ChemistryAtomic physicsRotational–vibrational couplingPeryleneJ-aggregatePeryleneFluorescent DyesThe Journal of Physical Chemistry A
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Calix[4]arene-functionalized naphthalene and perylene imide dyes.

2002

[reaction: see text] Calix[4]arenes bearing one, two, or four 1,8-naphthyl imide groups at the wide rim and bis-calix[4]arenes connected via perylene-bisimide dye spacers have been synthesized. The low-temperature NMR spectrum of the tetranaphthylimide suggests, in agreement with a crystal structure, a C2-symmetrical pinched cone conformation stabilized via face-to-face pi-pi interactions between opposite naphthylimide groups. UV-vis and fluorescence studies have been carried out for the perylene bis-calix[4]arene dyes.

Molecular StructureChemistryOrganic ChemistryCrystal structureNuclear magnetic resonance spectroscopyNaphthalenesPhotochemistryImidesBiochemistryFluorescencechemistry.chemical_compoundPhenolsPolymer chemistryCalixareneMoleculePhysical and Theoretical ChemistryCalixarenesImideColoring AgentsPerylenePeryleneNaphthaleneFluorescent DyesOrganic letters
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Recent advances in polyoxometalate-containing molecular conductors

2005

The recent advances in crystalline conducting molecular materials based on polyoxometalates (POMs) and organic donors of the tetrathiafulvalene (TTF) family or perylene are discussed. We emphasise the wide diversity of POM structural types and the variety of packing architectures for the organic molecules that can be induced by these inorganic anions. Besides structural effects, we show that these hybrids can have interesting electric and/or magnetic properties. Thus, in the last years the common belief that this type of radical salts containing such big and highly charged anions could only exhibit poor conducting properties has been refuted by the production of new materials exhibiting hig…

New materialsNanotechnologyOrganic moleculesInorganic ChemistryMetalchemistry.chemical_compoundchemistryvisual_artPolyoxometalateMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryMolecular materialsElectrical conductorTetrathiafulvalenePeryleneCoordination Chemistry Reviews
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Ultra-sensitive fluorescence spectroscopy of isolated surface-adsorbed molecules using an optical nanofiber.

2009

The strong radial confinement and the pronounced evanescent field of the guided light in optical nanofibers yield favorable conditions for ultra-sensitive surface spectroscopy of molecules deposited on the fiber. Using the guided mode of the nanofiber for both excitation and fluorescence collection, we present spectroscopic measurements on 3,4,9,10-perylenetetracarboxylic dianhydride molecules (PTCDA) at ambient conditions. Surface coverages as small as 1 per thousand of a compact monolayer still give rise to fluorescence spectra with a good signal to noise ratio. Moreover, we analyze and quantify the self-absorption effects due to reabsorption of the emitted fluorescence light by circumjac…

Optics and PhotonicsMaterials scienceOptical fiberLuminescenceSurface PropertiesFluorescence spectroscopyFluorescencelaw.inventionAnhydridesOpticslawMonolayerFiber Optic TechnologySpectroscopyLaser-induced fluorescencePeryleneOptical FibersTotal internal reflectionbusiness.industryLasersFluorescenceAtomic and Molecular Physics and OpticsSpectrometry FluorescenceAdsorptionLuminescencebusinessOptics express
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Theoretical determination of the geometric and electronic structures of oligorylenes and poli(peri‐naphthalene)

1992

We present a theoretical investigation of the electronic structure of oligorylenes (from perylene to heptarylene, including also the naphthalene molecule) and their corresponding polymer poly(peri‐naphthalene) (PPN) using the nonempirical valence effective (VEH) method. The geometry of the unit cell used to generate the polymer is extrapolated from the PM3‐optimized molecular geometries of the longest oligorylenes. That geometry shows some bond alternation along the perimeter carbon chains and a bond length of ≊1.46 Å is calculated for the peri bonds connecting the naphthalene units. The VEH one‐electron energy level distributions calculated for oligorylenes are used to interpret the experi…

OptimizationChemical BondsBand gapStereochemistryExtrapolationElectric ConductorsGeometryGeneral Physics and AstronomyElectronic structureMolecular physicsEnergy LevelsMolecular orbitalPhysical and Theoretical ChemistryBand Structure:FÍSICA::Química física [UNESCO]Electronic band structurePeryleneFilmsValence (chemistry)Organic PolymersChemistryElectronic Structure ; Perylene ; Naphthalene ; Organic Polymers ; Unit Cell ; Geometry ; Extrapolation ; Optimization ; Chemical Bonds ; Carbon ; Chains ; Energy Levels ; Ionization Potential ; Affinity ; Band Structure ; Electric Conductors ; Films ; PyrolysisUnit CellChainsCarbonUNESCO::FÍSICA::Química físicaBond lengthIonization PotentialMolecular geometryElectronic StructureAffinityIonization energyNaphthalenePyrolysis
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Fast and Efficient Microwave-Assisted Synthesis of Perylenebisimides

2015

Perylene-3,4,9,10-tetracarboxylic acid bisimides have been widely studied as industrial pigments. Lately, these dyes have drawn considerable attention because of applications as photocatalysts and organic semi-conductors. Here, we report a novel method for fast and efficient synthesis of many different perylenebisimides, based on microwave-assisted reactions.

Organic ChemistryDyes/pigmentAmines; Amino acids; Condensation reactions; Dyes/pigments; Microwave chemistry; PerylenebisimidesPerylenebisimidesPerylenebisimideAmino acidMicrowave chemistryCondensation reactionAmino acidsAmines; Amino acids; Condensation reactions; Dyes/pigments; Microwave chemistry; Perylenebisimides; Organic Chemistry; Physical and Theoretical ChemistryDyes/pigmentsAminesPhysical and Theoretical ChemistryCondensation reactionsAmine
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Energy Transfer at the Single-Molecule Level: Synthesis of a Donor-Acceptor Dyad from Perylene and Terrylene Diimides

2013

In 2004, we reported single-pair fluorescence resonance energy transfer (spFRET), based on a perylene diimide (PDI) and terrylene diimide (TDI) dyad (1) that was bridged by a rigid substituted para-terphenyl spacer. Since then, several further single-molecule-level investigations on this specific compound have been performed. Herein, we focus on the synthesis of this dyad and the different approaches that can be employed. An optimized reaction pathway was chosen, considering the solubilities, reactivities, and accessibilities of the building blocks for each individual reaction whilst still using established synthetic techniques, including imidization, Suzuki coupling, and cyclization reacti…

Organic ChemistryGeneral ChemistryChromophorePhotochemistryCatalysischemistry.chemical_compoundFörster resonance energy transferchemistrySuzuki reactionDiimideYield (chemistry)MoleculePeryleneDyadChemistry - A European Journal
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Efficient deep-red light-emitting electrochemical cells based on a perylenediimide-iridium-complex dyad

2009

A two-layer light-emitting electrochemical cell device based on a new perylenediimide-iridium-complex dyad is presented emitting in the deep-red region with high external quantum efficiencies (3.27%). Costa Riquelme, Ruben Dario, Ruben.Costa@uv.es ; Orti Guillen, Enrique, Enrique.Orti@uv.es ; Bolink, Henk, Henk.Bolink@uv.es ; Gierschner, Johannes, Johannes.Gierschner@uv.es

Organic light-emitting devicesMaterials scienceLightUNESCO::QUÍMICALight-emitting electrochemical cellschemistry.chemical_elementImidesIridium:QUÍMICA [UNESCO]CatalysisElectrochemical cellExternal quantum efficienciesElectrochemistryOrganometallic CompoundsMaterials ChemistryLight-emitting electrochemical cells ; Organic light-emitting devices ; Perylenediimide-iridium-complex ; External quantum efficienciesRed lightIridiumPerylenePhotonsLuminescent AgentsMolecular Structurebusiness.industryUNESCO::QUÍMICA::Química analíticaMetals and AlloysGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryLuminescent MeasurementsCeramics and Composites:QUÍMICA::Química analítica [UNESCO]OptoelectronicsPerylenediimide-iridium-complexbusiness
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Generation of white LED light by frequency downconversion using a perylene-based dye

2012

A high efficiency white light emitting diode (LED) was fabricated by generation of frequency down-conversion from a GaN/InGaN blue LED. In place of conventional inorganic phosphors, a perylene-based dye was used for colour conversion. The resulting hybrid structure is analysed by focusing on the visual performance of the realised LEDs employing the most relevant photometric parameters of a light source. Preparation of the organic polymer is described as well. The thermal stability of the dye was investigated and a simple structure which avoids colour degradation is proposed.

Organic polymerMaterials sciencebusiness.industryPhosphordyes light emitting diodes phosphors polymers wide band gap semiconductors GaN-InGaN blue LED colour conversionSettore ING-INF/01 - Elettronicalaw.inventionchemistry.chemical_compoundOpticsLight sourcechemistrylawOptoelectronicsDegradation (geology)Thermal stabilityElectrical and Electronic EngineeringbusinessPeryleneDiodeLight-emitting diode
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Spectroscopic characterization of red perylimide/surfactant nanocomposites

2011

Novel photoluminescent materials formed by some selected surfactants, metal derivatives of bis(2-ethylhexyl) sulfosuccinate (M(AOT)n; M = Na+, Co2+, Er3+ and Yb3+), bis(2-ethylhexyl) amine (BEEA), bis(2-ethylhexy1) phosphoric acid (HDEHP) and a 1:1 BEEA/HDEHP mixture, doped with the red perylimide (ROT-300) have been prepared, and their optical properties have been tested by absorption spectroscopy and steady state and timeresolved fluorescence. Experimental results show spectral shifts of the typical ROT-300 absorption and fluorescence bands with respect to that in apolar solvent medium. Data analysis leads consistently to attribute this feature mainly to the freezing of the diffusive move…

PERYLENEROT ASEMaterials sciencePhotoluminescenceDye laserMICELLESAbsorption spectroscopyDYEMechanical EngineeringAnalytical chemistryDNAFluorescenceMicelleMechanics of MaterialsLiquid crystalGeneral Materials ScienceLASERAbsorption (chemistry)LuminescenceSettore CHIM/02 - Chimica Fisica
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